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FDA 510(k) Applications Submitted by Ziehm-Orthoscan, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K250587
02/27/2025
Orthoscan TAU Mini C-Arm
Ziehm-Orthoscan, Inc.
K243452
11/07/2024
Orthoscan VERSA Mini C-Arm
Ziehm-Orthoscan, Inc.
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